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Qa document controller

Falkirk
Piramal Pharma Limited
Document controller
€30,000 a year
Posted: 4 May
Offer description

QA Document Controller page is loaded## QA Document Controllerremote type: Onsitelocations: Falkirktime type: Full timeposted on: Posted Todaytime left to apply: End Date: May 28, 2026 (29 days left to apply)job requisition id: R00000985***Be the First to Apply*****Division**Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit :Job TitleQA Document ControllerJob DescriptionDocument Controller - assist in day to day document control support service.Successful candidate will be responsible for :Issuing controlled copies of GMP documentationLogging and tracking of documents through QA deptProvide Document Control input including but not limited to mastering of documentation, issuing documentation to operative departments, scanning and archiving of completed documentationIf required, participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer related issues.Supply of controlled documents for use in audits of to support production and other support functions as required.Be involved in the preparation for customer and regulatory audits and inspectionsProvide document control support for the introduction of new products ensuring that all GMP documents are appropriate and all requirements are metAssist in the management of document transfer to off-site archive facility.Required Competencies :Attention to detailGood communication skills both verbal and writtenGood organisational skillsAbility to work effectively both individually and as part of a teamAbility to analyze data and information and make considered decisionsThe ability to identify root cause of problems to determine appropriate solutionsAbility to prioritize workload, follow instructions accurately and escalate issues as appropriate### Get In TouchIntroduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law.Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.
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